US10934284B2ActiveUtilityA1

Aminoquinazoline compounds having anti-inflammatory, antifungal, antiparasitic, and anticancer activity

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Assignee: WELLSTAT THERAPEUTICS CORPPriority: Feb 1, 2013Filed: Feb 26, 2019Granted: Mar 2, 2021
Est. expiryFeb 1, 2033(~6.6 yrs left)· nominal 20-yr term from priority
C07D 471/04C07D 241/44C07D 241/20C07D 239/42C07D 235/08C07D 233/60C07D 215/46C07D 215/44C07D 215/42C07D 215/40C07D 215/38C07D 213/74C07D 213/73A61P 33/02A61K 31/704A61K 31/555A61K 31/505A61K 31/4965A61K 31/475A61K 31/4745A61K 31/472A61K 31/4706A61K 31/4425A61K 31/44A61K 31/4164A61K 31/40A01N 43/60A01N 43/50A01N 43/42A61K 2300/00C07D 209/12A61K 31/4709A61K 31/437A61K 31/4184A01N 43/90A01N 43/54C07D 239/94A61K 31/517A61K 31/498A61P 35/00A61K 31/337C07D 401/12A61P 29/00A61P 31/10Y02A50/30Y02P20/582Y02A50/409Y02A50/411
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PatentIndex Score
2
Cited by
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References
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Claims

Abstract

Amine compounds having activity against inflammation, fungi, unicellular parasitic microorganisms, and cancer are described. The compounds contain a monocyclic, bicyclic, or tricyclic aromatic ring having one, two, or three ring nitrogen atoms.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A compound represented by Formula IB1 or a pharmaceutically acceptable salt thereof 
       
         
           
           
               
               
           
         
         wherein n is 1; 
         Q is absent; 
         R 1  is hydrogen or halo; and 
         R 7  is phenyl substituted by alkoxy having from 6 to 10 carbon atoms or phenoxy. 
       
     
     
       2. The compound or salt of  claim 1 , wherein the compound is selected from the group consisting of:
 N-[3-(Hexyloxy)benzyl]quinazolin-4-amine, 
 N-[3-(Decyloxy)benzyl]quinazolin-4-amine, 
 N-[4-(Decyloxy)benzyl]quinazolin-4-amine, 
 N-[4-(Hexyloxy)benzyl]quinazolin-4-amine. 
 
     
     
       3. A pharmaceutical composition comprising an effective amount of the compound or pharmaceutically acceptable salt of  claim 1  and a pharmaceutically acceptable carrier. 
     
     
       4. The compound or salt of  claim 1 , wherein the compound is N-(3-Phenoxybenzyl)quinazolin-4-amine. 
     
     
       5. A pharmaceutical composition comprising an effective amount of the compound or pharmaceutically acceptable salt of  claim 4  and a pharmaceutically acceptable carrier. 
     
     
       6. A method of inhibiting a fungus ex vivo, comprising contacting a surface or the fungus with the compound or pharmaceutically acceptable salt of  claim 1 . 
     
     
       7. A method of inhibiting a fungus ex vivo, comprising contacting a surface or the fungus with the compound or pharmaceutically acceptable salt of  claim 4 .

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